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Molecular determinants of myeloma bone disease and uses thereof

a bone disease and molecular determinant technology, applied in the field of multiple myeloma, can solve the problems of unelucidated mechanisms responsible for such impairment, and achieve the effects of increasing bone mass, increasing bone mass, and partial repair of lytic lesions

Inactive Publication Date: 2010-01-05
THE BOARD OF TRUSTEES OF THE UNIV OF ARKANSAS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0015]Results disclosed in the present invention indicate that blocking the production and / or secretion of DKK-1 and FRZB may prevent or reverse bone loss in multiple myeloma patients. Further applications may include using DKK-1 and FRZB inhibitors to prevent bone loss in the general population. Additionally, Wnt signaling has recently been shown to be critical for the self renewal capacity of hematopoietic stem cells. Furthermore, a bone marrow niche required for hepatic stellate cell proliferation is formed by mature osteoblasts. The block to Wnt signaling by DKK1 and FRZB could directly and indirectly impair hepatic stellate cell (HSC) proliferation and thus may partly account for the immunosuppression and anemia seen in multiple myeloma. Thus, blocking DKK1 and / or FRZB may also prevent or reverse the defect in hematopoiesis seen in most patients with myeloma.
[0021]The present invention is further directed to a method of preventing bone resorption and increasing bone formation in an individual. Such a method comprises blocking the activity of DKK1. This blocking of the DKK1 activity increases osteoblast numbers and reduces osteoclast activity, thereby preventing bone resorption and increasing bone formation in the individual.

Problems solved by technology

However, the mechanisms responsible for such impairment have not been elucidated.

Method used

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  • Molecular determinants of myeloma bone disease and uses thereof
  • Molecular determinants of myeloma bone disease and uses thereof
  • Molecular determinants of myeloma bone disease and uses thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

Patients

[0097]174 patients with newly diagnosed multiple myeloma, 16 patients with monoclonal gammopathy of undetermined significance, 9 with Waldenström's macroglobulinemia, and 45 normal persons were studied. Table 1 shows the characteristics of the patients with multiple myeloma.

[0098]

TABLE 1Myeloma patient characteristics and their relationship to MRI lesionsPVariablen / N%MRI = 1+MRI = 0valueAge ≧ 65 yr23 / 1691417 / 132 (12.9%) 6 / 36 (16.7%) 0.59*Caucasian147 / 169 87113 / 132 (85.6%) 33 / 36 (91.7%) 0.42*Female68 / 1694055 / 132 (41.7%)13 / 36 (36.1%)0.55Kappa light chain104 / 165 6379 / 128 (61.7%)24 / 36 (66.7%)0.59Lambda light chain61 / 1653749 / 128 (38.3%)12 / 36 (33.3%)0.59IgA subtype39 / 1692325 / 132 (18.9%)14 / 36 (38.9%) 0.012B2M ≧ 4 mg / L60 / 1693647 / 132 (35.6%)13 / 36 (36.1%)0.96CRP ≧ 4 mg / L12 / 166711 / 129 (8.5%) 1 / 36 (2.8%) 0.47*Creatinine ≧ 2 mg / dL19 / 1691116 / 132 (12.1%)3 / 36 (8.3%) 0.77*LDH ≧ 190 UI / L52 / 1693144 / 132 (33.3%) 8 / 36 (22.2%)0.20Albumin 23 / 1691419 / 132 (14.4%) 4 / 36 (11.1%) 0.79*Hgb 40 / 1692431 / 132 ...

example 2

Bone Imaging

[0099]Images were reviewed, without prior knowledge of gene expression data, using a Canon PACS (Picture Archiving and Cataloging System). MRI scans were performed on 1.5 Tesla GE Signa™ scanners. X-rays were digitized from film in accordance with American College of Radiology standards. MRI scans and x-rays were linked to the Canon PACS system using the ACR's DICOM (Digital Imaging and Communications in Medicine) standard. Imaging was done in accordance with manufacturers' specifications. MRI images were created with pre- and post-gadolinium T1-weighting and STIR (short-tau inversion recovery) weighting.

example 3

Plasma Cell Isolation and Gene Expression Profiling

[0100]Following Ficoll-Hypaque gradient centrifugation, plasma cells obtained from the bone marrow were isolated from the mononuclear cell fraction by immunomagnetic bead selection using a monoclonal mouse anti-human CD138 antibody (Miltenyi-Biotec, Auburn, Calif.). More than 90 percent of the cells used for gene expression profiling were plasma cells, as shown by two-color flow cytometry using CD138+ / CD45− and CD38+ / CD45− markers, the presence of cytoplasmic immunoglobulin light chains by immunocytochemistry, and morphology by Wright-Giemsa staining. Total RNA was isolated with RNeasy Mini Kit (Qiagen, Valencia, Calif.). Preparation of labeled cRNA and hybridization to U95Av2 microarrays containing approximately 10,000 genes (Affymetrix, Santa Clara, Calif.) was performed as previously described (Zhan et al., 2002; Zhan et al., 2003). RNA amplification was not required.

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Abstract

To identify molecular determinants of lytic bone disease in multiple myeloma, the expression profiles of ˜12,000 genes in CD138-enriched plasma cells from newly diagnosed multiple myeloma patients exhibiting no radiological evidence of lytic lesions (n=28) were compared to those with ≧3 lytic lesions (n=47). Two secreted WNT signaling antagonists, soluble frizzled related protein 3 (SFRP-3 / FRZB) and the human homologue of Dickkopf-1 (DKK1), were expressed in 40 of 47 with lytic bone lesions, but only 16 of 28 lacking bone lesions (P<0.05). DKK1 and FRZB were not expressed in plasma cells from 45 normal bone marrow donors or 10 Waldenstrom's macroglobulinemia, a related plasma cells malignancy that lacks bone disease. These data indicate that these factors are important mediators of multiple myeloma bone disease, and inhibitors of these proteins may be used to block bone disease.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This is a continuation-in-part of non-provisional application U.S. Ser. No. 10 / 727,461, filed Dec. 4, 2003, now U.S. Pat. No. 7,459,437 which claims benefit of provisional patent application U.S. Ser. No. 60 / 431,040, filed Dec. 5, 2002.FEDERAL FUNDING LEGEND[0002]This invention was created, in part, using funds from the federal government under National Cancer Institute grants CA55819 and CA97513. Consequently, the U.S. government has certain rights in this invention.BACKGROUND OF THE INVENTION[0003]1. Field of the Invention[0004]The present invention relates generally to the study of multiple myeloma. More specifically, the present invention relates to the identification and validation of molecular determinants of myeloma bone disease through comparative global gene expression profiling and employment of the SCID-rab mouse model for primary myeloma.[0005]2. Description of the Related Art[0006]Multiple myeloma (MM) is a rare, yet incurable...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): A61K39/395A61K38/17C07K16/18C12Q1/68
CPCA61K38/177C07K16/18C12Q1/6883C12Q1/6886C12N15/113C12Q2600/112C12Q2600/118C12Q2600/136
Inventor SHAUGHNESSY, JOHN D.
Owner THE BOARD OF TRUSTEES OF THE UNIV OF ARKANSAS
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